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FDADecember 21, 2020device

Portex Acapella DH Vibratory PEP Device - Product Usage: a single patient use device that provides Positive Expiratory Pressure (PEP) Therapy for patients who have Cystic Fibrosis, COPD, asthma, and lung diseases with secretory problems, and patients with atelectasis.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Shipping box may contain wrong model.

What to do

FDA enforcement status: Terminated

Brands named

smiths medical asdsmithssmiths medical

UPCs

50788942215304

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Portex Acapella DH Vibratory PEP Device - Product Usage: a single patient use device that provides Positive Expiratory Pressure (PEP) Therapy for patients who have Cystic Fibrosis, COPD, asthma, and lung diseases with secretory problems, and patients with atelectasis. — Recall Details · AllClear